Metal-Organic-Framework-Derived Bismuth Nanosheets for Electrochemical and Solar-Driven Electrochemical CO2 Reduction to FormateShow others and affiliations
2021 (English)In: ChemElectroChem, E-ISSN 2196-0216, Vol. 8, no 5, p. 880-886Article in journal (Refereed) Published
Abstract [en]
Electrochemical CO2 reduction is a promising way to achieve CO2 fixation and energy storage. However, it is a challenge to develop the potential electrocatalysts with excellent performance and selectivity. Herein, bismuth nanosheet arrays (Bi/CC-17) are prepared through an in situ electrochemical transformation strategy by use of Bi-based metal organic frameworks (MOFs) as the precursors, which are then attached on carbon cloth. The as-synthesized Bi/CC-17 nanosheet arrays achieve considerable partial current density of 45 mA cm−2 and remarkably high faradic efficiency of 98 % at the potential of −1.1 V versus RHE for the conversion of CO2 to formate, outperforming most previously reported electrocatalysts. In particular, the solar-driven In2O3/In2S3∥Bi two-electrode system with a In2O3/In2S3-based photoanode and typical Bi-based cathode achieves high faradaic efficiencies of ≥90 % for HCOOH formation, from −0.6 to −1.6 V versus the counter electrode (vs. CE). This work paves an avenue to develop MOF-derived electrocatalysts for sustainable conversion of CO2 into valuable chemicals.
Place, publisher, year, edition, pages
Wiley , 2021. Vol. 8, no 5, p. 880-886
Keywords [en]
bismuth nanosheets, CO2 reduction, electrocatalysts, formate, metal-organic frameworks, Bismuth, Carbon dioxide, Electrodes, Electrolysis, Energy storage, Formic acid, Indium compounds, Nanosheets, Organic polymers, Organometallics, Counter electrodes, Electrochemical transformation, Faradaic efficiencies, Faradic efficiency, Metalorganic frameworks (MOFs), Partial currents, Two-electrode systems, Valuable chemicals, Reduction
National Category
Materials Chemistry
Identifiers
URN: urn:nbn:se:kth:diva-304936DOI: 10.1002/celc.202001613ISI: 000613421700001Scopus ID: 2-s2.0-85100302036OAI: oai:DiVA.org:kth-304936DiVA, id: diva2:1612829
Note
QC 20211119
2021-11-192021-11-192022-06-25Bibliographically approved